grant

A novel physical activity metric predicts cognitive and brain aging and ADRD risk

Organization UNIVERSITY OF PITTSBURGH AT PITTSBURGHLocation PITTSBURGH, UNITED STATESPosted 1 Sept 2024Deadline 30 Jun 2027
NIHUS FederalResearch GrantFY202521+ years oldAD dementiaAD pathologyAD related dementiaADRDAccelerometerActivities of Daily LivingActivities of everyday lifeAdultAdult HumanAffectAgingAlzheimer Type DementiaAlzheimer disease dementiaAlzheimer risk factorAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's DiseaseAlzheimer's and related dementiasAlzheimer's biomarkerAlzheimer's dementia and related dementiaAlzheimer's dementia or related dementiaAlzheimer's disease and related dementiaAlzheimer's disease and related disordersAlzheimer's disease biological markerAlzheimer's disease or a related dementiaAlzheimer's disease or a related disorderAlzheimer's disease or related dementiaAlzheimer's disease pathologyAlzheimer's disease related dementiaAlzheimer's disease riskAlzheimer's pathologyAlzheimers DementiaAlzheimer’s biological markerAlzheimer’s disease biomarkerAmentiaAmmon HornAreaAttentionBaltimoreBiological MarkersBlood PlasmaBrainBrain Nervous SystemCell Communication and SignalingCell SignalingCerebellumClassificationClinicalCognitionCognitiveCognitive DisturbanceCognitive ImpairmentCognitive agingCognitive declineCognitive function abnormalCornu AmmonisDataData SetDementiaDepositDepositionDiagnosisDiseaseDisease ProgressionDisorderDisturbance in cognitionEarly identificationEncephalonEntropyFundingHealthHippocampusHumanImpaired cognitionImpairmentIndividualInterventionIntracellular Communication and SignalingInvestigatorsLanguageLesionLinkLongitudinal StudiesMT-bound tauMeasurementMeasuresMemoryMethodsModern ManMonitorMotorNerve DegenerationNeuron DegenerationOccipital lobeOlder PopulationOutcomePETPET ScanPET imagingPETSCANPETTParietal LobeParticipantPathologicPathologic ProcessesPathological ProcessesPathway interactionsPatient Self-ReportPatternPersonsPhasePhysical activityPhysiologicPhysiologicalPilot ProjectsPlasmaPlasma SerumPositron Emission Tomography Medical ImagingPositron Emission Tomography ScanPositron-Emission TomographyPosturePrimary Senile Degenerative DementiaProbabilityR-Series Research ProjectsR01 MechanismR01 ProgramRad.-PETResearchResearch GrantsResearch PersonnelResearch Project GrantsResearch ProjectsResearchersRestReticuloendothelial System, Serum, PlasmaRiskScienceSecondary toSelf-ReportSignal TransductionSignal Transduction SystemsSignalingSystemSystematicsTemporal LobeTestingTimeVisuospatialWhite Matter Hyperintensityabnormally aggregated tau proteinaccelerometryactivity monitoractivity trackeradulthoodagedaged brainaging brainalzheimer riskbio-markersbiologic markerbiological signal transductionbiomarkerbrain MR imagingbrain MRIbrain atrophybrain magnetic resonance imagingbrain volumecerebral MR imagingcerebral MRIcerebral atrophycerebral magnetic resonance imagingclinical significanceclinically significantcognitive abilitycognitive dysfunctioncognitive functioncognitive losscohortconnectomecortical atrophydaily living functiondaily living functionalitydata diversitydesigndesigningdisease riskdisorder riskdiverse dataexecutive controlexecutive functionfallsfilamentous tau inclusionfrontal cortexfrontal lobefunctional abilityfunctional capacitygray matterhippocampalinsightlong-term studylongitudinal outcome studiesmicrotubule associated protein tau aggregationmicrotubule associated protein tau depositmicrotubule bound taumicrotubule-bound taumild cognitive disordermild cognitive impairmentmoderate-to-vigorous physical activitymotor diseasemotor disordermotor dysfunctionneocorticalneural degenerationneurodegenerationneurodegenerativeneurological degenerationneuronal degenerationneurophysiologicalneurophysiologynext generationnoveloccipital cortexolder adultolder adulthoodolder groupsolder individualsolder personpaired helical filament of tauparietal cortexpathwaypilot studypositron emission tomographic (PET) imagingpositron emission tomographic imagingpositron emitting tomographypre-clinicalpreclinicalpreventpreventingprimary degenerative dementiaprogramsresponseself-aggregate tausenile dementia of the Alzheimer typesubstantia albasubstantia griseatautau PHFtau Proteinstau accumulationtau aggregatetau aggregationtau factortau fibrillizationtau filamenttau neurofibrillary tangletau oligomertau paired helical filamenttau polymerizationtau-tau interactiontemporal cortextime usevisual spatialwhite matterτ Proteinsτ aggregation
Sign up free to applyApply link · pipeline · email alerts
— or —

Get email alerts for similar roles

Weekly digest · no password needed · unsubscribe any time

Full Description

Project Summary
Low physical activity (PA) levels have been associated with elevated risk of Alzheimer’s dementia and

related disorders (ADRD). The bulk of this evidence has been derived from self-report measures of

PA and focused solely on PA volume and intensity. Objective PA assessment and quantifying

dynamics of continuous PA fluctuations over time using accelerometry may extend this area of

science by identifying early changes in functional capacity and emergent motor dysfunction, allowing

for a deeper understanding of how such changes are connected to brain aging and AD risk. We thus

developed a novel metric – “PA complexity” using the multiscale entropy (MSE) method to quantify

daily activity patterns by analyzing continuous accelerometer signals and apply this complexity

measure to a diverse older population in the Human Connectome Project – Connectomics in Brain

Aging and Dementia. This proposed study aims to (1) explore the associations between PA

complexity and cognitive function across multiple domains and risk of mild cognitive impairment (MCI)

and AD, (2) determine whether low PA complexity relates to AT(N) biomarker classifications and white

matter hyperintensities, (3) and examine whether low PA complexity is associated with brain atrophy.

This study is significant because (1) understanding the link between complexity of daily PA patterns,

cognitive function, and brain atrophy has the potential to yield new insights into the underlying

mechanisms connecting motor dysfunction to brain aging, (2) identifying altered complexity of activity

patterns as preclinical indicators of ADRD will suggest novel directions for tailored interventions to

further prevent or delay the onset of ADRD.

Grant Number: 5R03AG088612-02
NIH Institute/Center: NIH

Principal Investigator: Yurun Cai

Sign up free to get the apply link, save to pipeline, and set email alerts.

Sign up free →

Agency Plan

7-day free trial

Unlock procurement & grants

Upgrade to access active tenders from World Bank, UNDP, ADB and more — with email alerts and pipeline tracking.

$29.99 / month

  • 🔔Email alerts for new matching tenders
  • 🗂️Track tenders in your pipeline
  • 💰Filter by contract value
  • 📥Export results to CSV
  • 📌Save searches with one click
Start 7-day free trial →